交联和非交联水凝胶药物偶联物的天然纤维包膜:口服药物递送的创新设计

Utkarsh Bhutani, Saptarshi Majumdar
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引用次数: 11

摘要

近年来,对用于治疗应用的具有成本效益的天然生物产品的需求不断增长。在这项工作中,豆蔻皮被加工成水凝胶药物偶联物的保护罩。无籽豆蔻壳由粗纤维组成,并对包封的水凝胶药物基质提供有效的保护,防止降解。海藻酸钠(SA)和明胶是可生物降解的聚合物,萘普生钠(亲水性)和哌啶(疏水性)是模型药物。包在这种外壳中的聚合物-药物混合物经过设计,可以为这两种药物提供长时间的零级释放动力学。水凝胶药物缀合物经过仔细优化,以在最少或不使用交联剂的情况下实现控制释放。藻酸钠的粘度是以这样一种方式使用的,即合成不含交联剂的水凝胶-药物混合物可以成为现实。外壳在接近灭菌温度时也被发现是稳定的。这项研究不仅关注自然界中的一种可用资源,还展示了现代方法的作用,将这种资源(豆蔻皮)转化为携带药物分子的聚合物混合物的保护屏障。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Natural fibre envelope for cross-linked and non-cross-linked hydrogel-drug conjugates: Innovative design for oral drug delivery

Recent years have witnessed growing demand for cost-effective natural bioproducts for therapeutic applications. In this work, cardamom husk was processed and turned into a protective shield for the hydrogel-drug conjugate. The seedless cardamom husk comprises of crude fibers and offers effective protection to the encapsulated hydrogel-drug matrix against degradation. Sodium alginate (SA) and gelatin were the biodegradable polymers utilized, while naproxen sodium (hydrophilic) and piperine (hydrophobic) were used as model drugs. The polymer-drug blend encased in this husk was engineered to give a long hour, zero-order release kinetics for both types of drugs. The hydrogel-drug conjugate was carefully optimized to achieve a controlled release with minimal or no use of cross-linkers. The viscosity of sodium alginate was used in such a way that the synthesis of a cross-linker free hydrogel-drug blend can be a reality. The husk was also found to be stable near sterilization temperatures. This research not only focusses on an available resource in nature but also showcases the role of modern methodology to convert this resource (cardamom husk) into a protective shield for a polymeric blend carrying drug molecules.

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